A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4178780



Internal ID11461318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167940571..167940857hg38UCSC Ensembl
chr6:168341251..168341537hg19UCSC Ensembl
chr6:168084100..168084386hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38287
hg19287
hg18287
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1558245
Supporting Variants
SamplesHuRef
Known GenesMLLT4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4178780
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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